EPSPS mutants

ABSTRACT

The present invention relates to the production of a non-transgenic plant resistant or tolerant to a herbicide of the phosphonomethylglycine family, e.g., glyphosate. The present invention also relates to the use of a recombinagenic oligonucleobase to make a desired mutation in the chromosomal or episomal sequences of a plant in the gene encoding for 5-enol pyruvylshikimate-3-phosphate synthase (EPSPS). The mutated protein, which substantially maintains the catalytic activity of the wild-type protein, allows for increased resistance or tolerance of the plant to a herbicide of the phosphonomethylglycine family, and allows for the substantially normal growth or development of the plant, its organs, tissues or cells as compared to the wild-type plant irrespective of the presence or absence of the herbicide. Additionally the present invention relates to mutant  E. coli  cells that contain mutated EPSPS genes.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. patent application Ser. No. 13/621,662, filed Sep. 17, 2012, which is a divisional of U.S. patent application Ser. No. 12/160,725, filed Nov. 17, 2008, now U.S. Pat. No. 8,268,622, issued Sep. 18, 2012, which is the national stage application of International Application No. PCT/US2007/000591, filed Jan. 10, 2007, which claims the benefit of U.S. Provisional Application No. 60/758,439, filed Jan. 12, 2006, all of which are hereby incorporated by reference herein in their entirety, including any figures, tables, or drawings.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has been submitted in ASCII format via EFS-Web and is hereby incorporated by reference in its entirety. Said ASCII copy, created on Jul. 19, 2018, is named CIBUS-007-CT_SeqListing.txt and is 25 kilobytes in size.

FIELD OF THE INVENTION

The present invention relates to the production of a non-transgenic plant resistant or tolerant to an herbicide of the phosphonomethylglycine family, e.g., glyphosate. The present invention also relates to the use of a recombinagenic oligonucleobase to make a desired mutation in the chromosomal or episomal sequences of a plant in the gene encoding for 5-enol pyruvylshikimate-3-phosphate synthase (EPSPS). The mutated protein, which substantially maintains the catalytic activity of the wild-type protein, allows for increased resistance or tolerance of the plant to a herbicide of the phosphonomethylglycine family, and allows for the substantially normal growth or development of the plant, its organs, tissues or cells as compared to the wild-type plant regardless of the presence or absence of the herbicide. The present invention also relates to an E. coli cell having a mutated EPSPS gene, a non-transgenic plant cell in which the EPSPS gene has been mutated, a non-transgenic plant regenerated therefrom, as well as a plant resulting from a cross using a regenerated non-transgenic plant having a mutated EPSPS gene as one of the parents of the cross. The present mutated EPSPS protein has been changed in amino acid positions 159, 178, 182, 193, 244, 273 and/or 454 in the Arabidopsis EPSPS protein (NM 130093) or at an analogous amino acid residue in an EPSPS paralog.

BACKGROUND OF THE INVENTION

Phosphonomethylglycine Herbicides

Herbicide-tolerant plants may reduce the need for tillage to control weeds thereby effectively reducing soil erosion. One herbicide which is the subject of much investigation in this regard is N-phosphonomethylglycine, commonly referred to as glyphosate. Glyphosate inhibits the shikimic acid pathway which leads to the biosynthesis of aromatic compounds including amino acids, hormones and vitamins. Specifically, glyphosate curbs the conversion of phosphoenolpyruvic acid (PEP) and 3-phosphoshikimic acid to 5-enolpyruvyL-3-phosphoshikimic acid by inhibiting the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (hereinafter referred to as EPSP synthase or EPSPS). For purposes of the present invention, the term “glyphosate” includes any herbicidally effective form of N-phosphonomethylglycine (including any salt thereof), other forms which result in the production of the glyphosate anion in plants and any other herbicides of the phosphonomethlyglycine family.

Tolerance of plants to glyphosate can be increased by introducing a mutant EPSPS gene having an alteration in the EPSPS amino acid coding sequence into the genome of the plant. Examples of some of the mutations in the EPSPS gene for inducing glyphosate tolerance are described in the following patents: U.S. Pat. Nos. 5,310,667; 5,866,775; 5,312,910; 5,145,783. These proposed mutations typically have a higher K₁ for glyphosate than the wild-type EPSPS enzyme which confers the glyphosate-tolerant phenotype, but these variants are also characterized by a high K_(m) for PEP which makes the enzyme kinetically less efficient (Kishore et al., 1998, Ann. Rev. Biochem. 57:627-663; Schulz et al., 1984, Arch. Microbiol. 137:121-123; Sost et al., 1984, FEBS Lett. 173:238-241; Kishore et al., 1986, Fed. Proc. 45: 1506; Sost and Amrhein, 1990, Arch. Biochem. Biophys. 282: 433-436). Many mutations of the EPSPS gene are chosen so as to produce an EPSPS enzyme that is resistant to herbicides, but unfortunately, the EPSPS enzyme produced by the mutated EPSPS gene has a significantly lower enzymatic activity than the wild-type EPSPS. For example, the apparent K_(m) for PEP and the apparent K₁ for glyphosate for the wild-type EPSPS from E. coli are 10 μM and 0.5 μM, respectively, while for a glyphosate-tolerant isolate having a single amino acid substitution of alanine for glycine at position 96, these values are 220 μM and 4.0 mM, respectively. A number of glyphosate-tolerant EPSPS genes have been constructed by mutagenesis. Again, the glyphosate-tolerant EPSPS had lower catalytic efficiency (V_(max)/K_(m)), as shown by an increase in the K_(m) for PEP, and a slight reduction of the V_(max) of the wild-type plant enzyme (Kishore et al., 1998, Ann. Rev. Biochem. 57:627-663).

Since the kinetic constants of the variant enzymes are impaired with respect to PEP, it has been proposed that high levels of overproduction of the variant enzyme, 40-80 fold, would be required to maintain normal catalytic activity in plants in the presence of glyphosate (Kishore et al., 1988, Ann. Rev. Biochem. 57:627-663). It has been shown that glyphosate-tolerant plants can be produced by inserting into the genome of the plant the capacity to produce a higher level of EPSP synthase in the chloroplast of the cell (Shah et al., 1986, Science 233, 478-481), which enzyme is preferably glyphosate-tolerant (Kishore et al., 1988, Ann. Rev. Biochem. 57:627-663).

The introduction of the exogenous mutant EPSPS genes into plant is well documented. For example, according to U.S. Pat. No. 4,545,060, to increase a plant's resistance to glyphosate, a gene coding for an EPSPS variant having at least one mutation that renders the enzyme more resistant to its competitive inhibitor, i.e., glyphosate, is introduced into the plant genome. However, many complications and problems are associated with these transgenic plants containing mutant EPSPS genes. Many such mutations result in low expression of the mutated EPSPS gene product or result in an EPSPS gene product with significantly lower enzymatic activity as compared to wild type. The low expression or low enzymatic activity of the mutated enzyme results in abnormally low levels of growth and development of the plant.

While such variants in the EPSP synthases have proved useful in obtaining transgenic plants tolerant to glyphosate, it would be increasingly beneficial to obtain a variant EPSPS gene product that is highly glyphosate-tolerant but still kinetically efficient, such that improved tolerance can be obtained with a wild-type expression level.

Recombinagenic Oligonucleobases

Recombinagenic oligonucleobases and their use to effect genetic changes in eukaryotic cells are described in U.S. Pat. No. 5,565,350 to Kmiec (Kmiec I). Kmiec I teaches a method for introducing specific genetic alterations into a target gene. Kmiec I discloses, inter alia, recombinagenic oligonucleobases having two strands, in which a first strand contains two segments of at least 8 RNA-like nucleotides that are separated by a third segment of from 4 to about 50 DNA-like nucleotides, termed an “interposed DNA segment.” The nucleotides of the first strand are base paired to DNA-like nucleotides of a second strand. The first and second strands are additionally linked by a segment of single stranded nucleotides so that the first and second strands are parts of a single oligonucleotide chain. Kmiec I further teaches a method for introducing specific genetic alterations into a target gene. According to Kmiec I, the sequences of the RNA segments are selected to be homologous, i.e., identical, to the sequence of a first and a second fragment of the target gene. The sequence of the interposed DNA segment is homologous with the sequence of the target gene between the first and second fragment except for a region of difference, termed the “heterologous region.” The heterologous region can effect an insertion or deletion, or can contain one or more bases that are mismatched with the sequence of target gene so as to effect a substitution. According to Kmiec I, the sequence of the target gene is altered as directed by the heterologous region, such that the target gene becomes homologous with the sequence of the recombinagenic oligonucleobase. Kmiec I specifically teaches that ribose and 2′-O-methylribose, i.e., 2′-methoxyribose, containing nucleotides can be used in recombinagenic oligonucleobases and that naturally-occurring deoxyribose-containing nucleotides can be used as DNA-like nucleotides.

U.S. Pat. No. 5,731,181 to Kmiec (Kmiec II) specifically disclose the use of recombinagenic oligonucleobases to effect genetic changes in plant cells and discloses further examples of analogs and derivatives of RNA-like and DNA-like nucleotides that can be used to effect genetic changes in specific target genes. Other patents discussing the use of recombinagenic oligonucleobases include: U.S. Pat. Nos. 5,756,325; 5,871,984; 5,760,012; 5,888,983; 5,795,972; 5,780,296; 5,945,339; 6,004,804; and 6,010,907 and in International Patent No. PCT/US00/23457; and in International Patent Publication Nos. WO 98/49350; WO 99/07865; WO 99/58723; WO 99/58702; and WO 99/40789. Recombinagenic oligonucleobases include mixed duplex oligonucleotides, non-nucleotide containing molecules taught in Kmiec II and other molecules taught in the above-noted patents and patent publications.

U.S. Pat. No. 6,870,075 ('075 patent) discloses a method for producing a non-transgenic, herbicide resistant or tolerant plants employing recombinagenic oligonucleobases according to the methods disclosed in Kmiec I and Kmiec II. The EPSPS mutants disclosed in the '075 patent include changes made in the following amino acid positions of the EPSPS protein: Leu₁₇₃, Gly₁₇₇, Thr₁₇₈, Ala₁₇₉, Met₁₈₀, Arg₁₈₁, Pro₁₈₂, Ser₉₈, Ser₂₅₅ and Leu₁₉₈ in the Arabidopsis EPSPS protein or at an analogous amino acid residue in an EPSPS paralog.

Published US Patent Application 20030084473 also discloses the use of recombinagenic oligonucleobases to make non-transgenic herbicide resistant plants where the EPSPS protein has been changed in amino acid positions 126, 177, 207, 438, 479, 480 and/or 505 in the Arabidopsis EPSPS protein or at an analogous amino acid residue in an EPSPS paralog.

The present invention relates to additional amino acid mutations that can be made in any EPSPS gene from any species to produce a gene product that possesses resistance to glyphosate.

SUMMARY OF THE INVENTION

Briefly, in accordance with the present invention, a non-transgenic plant or plant cell having one or more mutations in the EPSPS gene is made. The resulting plant has increased resistance or tolerance to a member of the phosphonomethylglycine family such as glyphosate and exhibits substantially normal growth or development of the plant, its organs, tissues or cells, as compared to the corresponding wild-type plant or cell. The mutated gene produces a gene product having a substitution at one or more of the amino acid positions 160, 179, 183, 194, 244, 273 and/or 454 in the Arabidopsis EPSPS protein (AF360224) or at an analogous amino acid residue in an EPSPS paralog. Preferably, the mutated plant is resistant to glyphosate and has substantially the same catalytic activity as compared to the wild-type EPSPS protein.

Additionally, the present invention includes a mutated EPSPS gene from an E coli and mutated E coli cells that produces a gene product having a substitution at one or more of the amino acid positions 82, 97, 101, 114, 164, 193 and 374. The mutated E coli EPSPS gene can be used for in vitro testing of the mutated gene product. Once active E coli mutants have been identified then corresponding mutants can then be made to an EPSPS gene in a desirable crop to impart herbicide resistance to the crop.

The present invention also relates to a method for producing a non-transgenic plant having a mutated EPSPS gene that substantially maintains the catalytic activity of the wild-type protein regardless of the presence or absence of a herbicide of the phosphonomethylglycine family. The method comprises introducing into a plant cell a recombinagenic oligonucleobase with a targeted mutation in the EPSPS gene that produces a gene product having one or more of the aforementioned amino acid changes. The method further includes identifying a cell, seed, or plant having a mutated EPSPS gene and to culturing and regeneration methods to obtain a plant that produces seeds, henceforth a “fertile plant”, and the production of seeds and additional plants from such a fertile plant including descendant (progeny) plants that contain the mutated EPSPS gene.

The invention is further directed to a method of selectively controlling weeds in a field. The field comprises plants with the disclosed EPSPS gene alterations and weeds. The method comprises application to the field of a phospnomethyglycine herbicide to which the said plants are rendered resistant and the weeds are controlled. A preferred herbicide is glyphosate.

The invention is also directed to novel mutations in the EPSPS gene and resulting novel gene product that confer resistance or tolerance to a member of the phosphonomethylglycine family, e.g., glyphosate, to a plant or wherein the mutated EPSPS has substantially the same enzymatic activity as compared to wild-type EPSPS. Additionally, the present invention is directed to a mutated E. coli EPSPS gene product (protein) that is used to screen EPSPS mutants for use as herbicide resistant mutations in plants.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows the EPSPS gene (AroA gene) product protein sequence (SEQ ID NO: 17) in E. Coli where the mutated amino acid positions are depicted with a box around them. The substituted amino acid in those positions is shown below the sequence.

FIG. 2 shows the protein sequence (SEQ ID NO: 18) of AtEPSPS cDNA-At2g45300 translated from Genbank accession NM_130093 (Arabodopsis).

FIG. 3 shows the protein sequence (SEQ ID NO: 19) of AtEPSPS cDNA-At1g48860 translated from Genbank accession AF360224T (Arabodopsis).

FIG. 4 shows the protein sequence (SEQ ID NO: 20) of BnEPSPS cDNA-BN-2 2-23 (Canola).

FIG. 5 shows the protein sequence (SEQ ID NO: 21) of BnEPSPS cDNA-2-28 from X51475 gDNA translation (Canola).

DETAILED DESCRIPTION OF THE INVENTION

Definitions

The invention is to be understood in accordance with the following definitions.

An oligonucleobase is a polymer of nucleobases, which polymer can hybridize by Watson-Crick base pairing to a DNA having the complementary sequence.

Nucleobases comprise a base, which is a purine, pyrimidine, or a derivative or analog thereof. Nucleobases include peptide nucleobases, the subunits of peptide nucleic acids, and morpholine nucleobases as well as nucleosides and nucleotides. Nucleosides are nucleobases that contain a pentosefuranosyl moiety, e.g., an optionally substituted riboside or 2′-deoxyriboside. Nucleosides can be linked by one of several linkage moieties, which may or may not contain a phosphorus. Nucleosides that are linked by unsubstituted phosphodiester linkages are termed nucleotides.

An oligonucleobase chain has a single 5′ and 3′ terminus, which are the ultimate nucleobases of the polymer. A particular oligonucleobase chain can contain nucleobases of all types. An oligonucleobase compound is a compound comprising one or more oligonucleobase chains that are complementary and hybridized by Watson-Crick base pairing. Nucleobases are either deoxyribo-type or ribo-type. Ribo-type nucleobases are pentosefuranosyl containing nucleobases wherein the 2′ carbon is a methylene substituted with a hydroxyl, alkyloxy or halogen. Deoxyribo-type nucleobases are nucleobases other than ribo-type nucleobases and include all nucleobases that do not contain a pentosefuranosyl moiety.

An oligonucleobase strand generically includes both oligonucleobase chains and segments or regions of oligonucleobase chains. An oligonucleobase strand has a 3′ end and a 5′ end. When a oligonucleobase strand is coextensive with a chain, the 3′ and 5′ ends of the strand are also 3′ and 5′ termini of the chain.

According to the present invention, substantially normal growth of a plant, plant organ, plant tissue or plant cell is defined as a growth rate or rate of cell division of the plant, plant organ, plant tissue, or plant cell that is at least 35%, at least 50%, at least 60%, or at least 75% of the growth rate or rate of cell division in a corresponding plant, plant organ, plant tissue or plant cell expressing the wild type EPSPS protein.

According to the present invention, substantially normal development of a plant, plant organ, plant tissue or plant cell is defined as the occurrence of one or more developmental events in the plant, plant organ, plant tissue or plant cell that are substantially the same as those occurring in a corresponding plant, plant organ, plant tissue or plant cell expressing the wild type EPSPS protein.

According to the present invention plant organs include, but are not limited to, leaves, stems, roots, vegetative buds, floral buds, meristems, embryos, cotyledons, endosperm, sepals, petals, pistils, carpels, stamens, anthers, microspores, pollen, pollen tubes, ovules, ovaries and fruits, or sections, slices or discs taken therefrom. Plant tissues include, but are not limited to, callus tissues, ground tissues, vascular tissues, storage tissues, meristematic tissues, leaf tissues, shoot tissues, root tissues, gall tissues, plant tumor tissues, and reproductive tissues. Plant cells include, but are not limited to, isolated cells with cell walls, variously sized aggregates thereof, and protoplasts.

Plants are substantially “tolerant” to glyphosate when they are subjected to it and provide a dose/response curve which is shifted to the right when compared with that provided by similarly subjected non-tolerant like plant. Such dose/response curves have “dose” plotted on the X-axis and “percentage kill”, “herbicidal effect”, etc., plotted on the y-axis. Tolerant plants will require more herbicide than non-tolerant like plants in order to produce a given herbicidal effect. Plants which are substantially “resistant” to the glyphosate exhibit few, if any, necrotic, lytic, chlorotic or other lesions, when subjected to glyphosate at concentrations and rates which are typically employed by the agrochemical community to kill weeds in the field. Plants which are resistant to a herbicide are also tolerant of the herbicide. The terms “resistant” and “tolerant” are to be construed as “tolerant and/or resistant” within the context of the present application.

The term “EPSPS homolog” or any variation therefore refers to an EPSPS gene or EPSPS gene product found in another plant species that performs the same or substantially the same biological function as the EPSPS genes disclosed herein and where the nucleic acid sequences or polypeptide sequences (of the EPSPS gene product) are said to be “identical” or at least 50% similar (also referred to as ‘percent identity’ or ‘substantially identical’) as described below. Two polynucleotides or polypeptides are identical if the sequence of nucleotides or amino acid residues, respectively, in the two sequences is the same when aligned for maximum correspondence as described below. The terms “identical” or “percent identity,” in the context of two or more nucleic acids or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or nucleotides that are the same, when compared and aligned for maximum correspondence over a comparison window, as measured using one of the following sequence comparison algorithms or by manual alignment and visual inspection. For polypeptides where sequences differ in conservative substitutions, the percent sequence identity may be adjusted upwards to correct for the conservative nature of the substitution. Means for making this adjustment are well known to those of skill in the art. Typically this involves scoring a conservative substitution as a partial rather than a full mismatch, thereby increasing the percentage sequence identity. Thus, for example, where an identical amino acid is given a score of 1 and a non-conservative substitution is given a ‘score of zero, a conservative substitution is given a score between zero and 1. The scoring of conservative substitutions is calculated according to, e.g., the algorithm of Meyers & Miller, Computer Applic. Biol. Sci. 4: 11-17 (1988) e.g., as implemented in the program PC/GENE (Intelligenetics, Mountain View, Calif., USA).

The phrases “substantially identical,” and “percent identity” in the context of two nucleic acids or polypeptides, refer to sequences or subsequences that have at least 50%, advantageously 60%, preferably 70%, more preferably 80%, and most preferably 90-95% nucleotide or amino acid residue identity when aligned for maximum correspondence over a comparison window as measured using one of the following sequence comparison algorithms or by manual alignment and visual inspection. This definition also refers to the complement of a test sequence, which has substantial sequence or subsequence complementarity when the test sequence has substantial identity to a reference sequence.

One of skill in the art will recognize that two polypeptides can also be “substantially identical” if the two polypeptides are immunologically similar. Thus, overall protein structure may be similar while the primary structure of the two polypeptides display significant variation. Therefore a method to measure whether two polypeptides are substantially identical involves measuring the binding of monoclonal or polyclonal antibodies to each polypeptide. Two polypeptides are substantially identical if the antibodies specific for a first polypeptide bind to a second polypeptide with an affinity of at least one third of the affinity for the first polypeptide. For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are input into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. The sequence comparison algorithm then calculates the percent sequence identity for the test sequence(s) relative to the reference sequence, based on the designated program parameters.

Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith & Waterman, 0.4dv. Appl. Math. 2:482 (I 98 I), by the homology alignment algorithm of Needleman & Wunsch, J. Mol. Biol. 48:443 (1970), by the search for similarity method of Pearson & Lipman, Proc. Nat'l. Acad. Sci. USA 5 85:2444 (1988), by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.), by software for alignments such as VECTOR NTI Version #6 by InforMax, Inc. MD, USA, by the procedures described in ClustalW, Thompson, J. D., Higgins, D. G. and Gibson, T. J. (1994) CLUSTALW: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position—specific gap penalties and weight matrix choice. Nucleic Acids Research, 22:4673-4680 or by visual inspection (see generally, Protocols in Molecular Biology, F. M. Ausubel et al., eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc. and John Wiley & Sons, Inc., (1995 Supplement) (Ausubel)).

Examples of algorithms that are suitable for determining percent sequence identity and sequence similarity are the BLAST and BLAST 2.0 algorithms, which are described in Altschul et al. (1990) J. Mol. Biol. 215: 403-410 and Altschul et al. (1977) Nucleic Acids Res. 25: 33 89-3402, respectively. Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov/). This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al, supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are then extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always>0) and N (penalty score for mismatching residues; always<0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a word length (W) of 11, an expectation (E) of 10, M=5, N=−4, and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a word length (W) of 3, an expectation (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff& Henikoff, Proc. Natl. Acad. Sci. USA 89:10915 (1989)). In addition to calculating percent sequence identity, the BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin & Altschul, Proc. Nat'l. Acad. Sci. USA 90:5873-5787 (1993)). One measure of similarity provided by the BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid is considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.1, more preferably less than about 0.01, and most preferably less than about 0.001.

In practicing the present invention a non-transgenic plant or plant cell having one or more mutations in the EPSPS gene is made. The resulting plant has increased resistance or tolerance to a member of the phosphonomethylglycine family such as glyphosate and exhibits substantially normal growth or development of the plant, its organs, tissues or cells, as compared to the corresponding wild-type plant or cell. The mutated gene produces a gene product having a substitution at one or more of the amino acid positions 160, 179, 183, 194, 244, 273 and 454 of the Arabidopsis EPSPS gene AF 360244 product or at an analogous amino acid position in an EPSPS homolog. Preferably, the mutated plant is resistant to glyphosate and has substantially the same catalytic activity as compared to the wild-type EPSPS protein.

To identify mutant EPSPS genes that will produce a gene product that provides resistance to glyphosate, in vitro screening can be done in a bacterial system to save time and resources. Growth curves of bacterial colonies expressing candidate mutant EPSPS genes can be generated to evaluate the mutant EPSPS genes in providing a glyphosate resistant phenotype. For example, U.S. Pat. No. 6,870,075 discloses a Salmonella glyphosate resistance assay employing Arabidopsis mutant EPSPS genes transformed into a LacZ-Salmonella typhi strain. In another embodiment of the present invention, the E coli EPSPS gene, also called the AroA gene, can be used to evaluate EPSPS mutants for glyphosate resistance. Growth curve assays and enzymatic assays measuring K_(i) and K_(m) values for candidate mutants are conducted according to well known assay techniques. Once an active glyphosate resistant mutant is identified in E coli EPSPS gene then an analogous amino acid in a plant EPSPS gene is mutated with recombinagenic nucleobases as described herein to make a glyphosate resistant plant.

Preferred amino acid substitutions in the E. coli EPSPS gene (AroA) product include the following:

-   Leu₈₂Ser -   Thr₉₇Ile or Ala -   Pro₁₀₁Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₃₇₄LeU     wherein the amino acid to the left of the subscript number is the     native amino acid and the amino acid to the right of the subscript     number is the mutant amino acid. The letter “X” in amino acid     position 374 is designated because in the E. coli EPSPS gene product     the native amino acid is Leu. However, it has been discovered that     in many plant species the amino acid present in position 374 is not     Leu and when this position is changed to Leu the plant will exhibit     glyphosate resistance and will retain sufficient enzymatic activity     to support normal plant growth.

Corresponding amino acid positions in plant species are changed according to the present invention to produce a non-transgenic herbicide resistant plant. Below is a list of some preferred crops which list the amino acid positions in the EPSPS gene to be changed. Preferred amino acid substitutions are listed to the right of the amino acid position number.

For maize the following amino acid changes are preferred:

-   Leu₈₄Ser -   Thr₁₀₂Ile or Ala -   Pro₁₀₆Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₁₇Leu

For cotton the following amino acid changes are preferred:

-   Leu₈₂Ser -   Thr₉₇Ile or Ala -   Pro₁₇₃Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₈₄Leu

For rice the following amino acid changes are preferred

-   Leu₁₅₀Ser -   Thr₁₆₉Ile or Ala -   Pro₁₇₃Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₈₄Leu

For Brassica napus (2-28 from X51475 gDNA translation) the following amino acid changes are preferred:

-   Leu₁₅₅Ser -   Thr₁₇₄Ile or Ala -   Pro₁₇₈Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₈₉Leu

For Arabidopsis thaliana (AF360224) the following amino acid changes are preferred:

-   Leu₁₆₀Ser -   Thr₁₇₉Ile or Ala -   Pro₁₈₃Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₉₄Leu

For Petunia hybrida the following amino acid changes are preferred:

-   Leu₁₅₅Ser -   Thr₁₇₄Ile or Ala -   Pro₁₇₈Ala or Thr or Leu or Cys or Gly -   Val₁₁₄Ala -   Asp₁₆₄Ala -   Asn₁₉₃Ala and -   X₁₈₉Leu

As will be appreciated, E. coli is not a plant however it is contemplated in the present invention because the E. coli gene can be mutated in a bacterial cell culture system and then the mutated E. coli gene product (enzyme) can be assayed for enzymatic activity (K_(l) and K_(m)) that will indicate resistance to glyphosate and function as a necessary enzyme product which is essential in plants. Once a mutated E. coli mutant is identified then that mutation is made in a plant cell employing the recombinagenic oligonucleobases described herein to produce a non-transgenic herbicide resistant plant. For these reasons mutated E coli and mutated Area proteins are considered part of the present invention.

The following table lists preferred amino acid substitution positions, by amino acid number, for various species. Making amino acid substitutions at one or more of these positions will produce glyphosate resistant plants:

Genbank Protein Accession # L82 T97 P101 N111 E. coli X00557 82 97 101  111* Arabidopsis AF360224 160 179 183 194 thaliana Petunia hybrida M21084.1 155 174 178 189 Brassica napus X51475.1 155 174 178 189 Zea mays X63374 84 102 106 117 Oryza sativa AF413082 150 169 173 184 Arabidopsis NM 130093 159 178 182 193 thaliana *No true E. coli homologous amino acid

As can be seen from the above table and FIG. 1-5 there are some minor variations among the EPSPS genes between species and within species. This is to be expected. These minor variations should be taken into account when making mutants according to the present invention. Amino acids in analogous positions between the different genes are mutated to make glyphosate resistant plants. For example, the mutation in Arabidopsis AF360224 at position 179 (T>A) would be equivalent to a T>A mutation at position 178 in Arabidopsis NM 130093. Another example is seen in position L82 in the E coli EPSPS gene. Most plants have an L in the analgous position but Arabidopsis has an F the analogous at 159 or 160 depending on the Arabidopsis gene as indicated in the above table.

Additionally, some species have more than one EPSPS gene. In such a case one or more of the genes are mutated according to the present invention to make a glyphosate resistant mutant. If the expression levels of the various EPSPS genes is known and is different then it is preferred to mutate the higher expressing EPSPS genes. In a preferred embodiment all of the EPSPS genes in a crop are mutated to make a glyphosate phenotype. For example, canola is known to have four EPSPS genes. Two genes are shown in FIGS. 4 and 5. A comparison will show a light difference between the two genes.

The plant mutated according to the present invention can be of any species of dicotyledonous, monocotyledonous or gymnospermous plant, including any woody plant species that grows as a tree or shrub, any herbaceous species, or any species that produces edible fruits, seeds or vegetables, or any species that produces colorful or aromatic flowers. For example, the plant may be selected from a species of plant from the group consisting of canola, sunflower, tobacco, sugar beet, sweet potato, yam, cotton, maize, wheat, barley, rice, sorghum, tomato, mango, peach, apple, pear, strawberry, banana, melon, potato, carrot, lettuce, onion, soya spp, sugar cane, pea, peanut, field beans, poplar, grape, citrus, alfalfa, rye, oats, turf and forage grasses, flax, oilseed rape, cucumber, morning glory, balsam, pepper, eggplant, marigold, lotus, cabbage, daisy, carnation, tulip, iris, lily, and nut producing plants insofar as they are not already specifically mentioned.

The recombinagenic oligonucleobase can be introduced into a plant cell using any method commonly used in the art, including but not limited to, microcarriers (biolistic delivery), microfibers (whiskers), electroporation, direct DNA uptake and microinjection.

Illustrative examples of a recombinagenic oligonucleobase are described below.

The invention can be practiced with recombinagenic oligonucleobases having the conformations and chemistries described in the Kmiec I and Kmiec II patents which are incorporated herein by reference. Kmiec I teaches a method for introducing specific genetic alterations into a target gene. The recombinagenic oligonucleobases in Kmiec I and/or Kmiec II contain two complementary strands, one of which contains at least one segment of RNA-type nucleotides (an “RNA segment”) that are base paired to DNA-type nucleotides of the other strand.

Kmiec II discloses that purine and pyrimidine base-containing non-nucleotides can be substituted for nucleotides. U.S. Pat. Nos. 5,756,325; 5,871,984; 5,760,012; 5,888,983; 5,795,972; 5,780,296; 5,945,339; 6,004,804; and 6,010,907 and in International Patent No. PCT/US00/23457; and in International Patent Publication Nos. WO 98/49350; WO 99/07865; WO 99/58723; WO 99/58702; WO 99/40789; U.S. Pat. No. 6,870,075; and US Published Patent Application 20030084473, which are each hereby incorporated in their entirety, disclose additional recombinagenic molecules that can be used for the present invention. The term “recombinagenic oligonucleobase” is used herein to denote the molecules that can be used in the methods of the present invention and include mixed duplex oligonucleotides, non-nucleotide containing molecules taught in Kmiec II, single stranded oligodeoxynucleotides and other recombinagenic molecules taught in the above noted patents and patent publications.

In one embodiment, the recombinagenic oligonucleobase is a mixed duplex oligonucleotide in which the RNA-type nucleotides of the mixed duplex oligonucleotide are made RNase resistant by replacing the 2′-hydroxyl with a fluoro, chloro or bromo functionality or by placing a substituent on the 2′-O. Suitable substituents include the substituents taught by the Kmiec II. Alternative substituents include the substituents taught by U.S. Pat. No. 5,334,711 (Sproat) and the substituents taught by patent publications EP 629 387 and EP 679 657 (collectively, the Martin Applications), which are incorporated herein by reference. As used herein, a 2′-fluoro, chloro or bromo derivative of a ribonucleotide or a ribonucleotide having a 2′-OH substituted with a substituent described in the Martin Applications or Sproat is termed a “2′-Substituted Ribonucleotide.” As used herein the term “RNA-type nucleotide” means a 2′-hydroxyl or 2′-Substituted Nucleotide that is linked to other nucleotides of a mixed duplex oligonucleotide by an unsubstituted phosphodiester linkage or any of the non-natural linkages taught by Kmiec I or Kmiec II. As used herein the term “deoxyribo-type nucleotide” means a nucleotide having a 2′-H, which can be linked to other nucleotides of a MDON by an unsubstituted phosphodiester linkage or any of the non-natural linkages taught by Kmiec I or Kmiec II.

In one embodiment of the present invention, the recombinagenic oligonucleobase is a mixed duplex oligonucleotide that is linked solely by unsubstituted phosphodiester bonds. In alternative embodiments, the linkage is by substituted phosphodiesters, phosphodiester derivatives and non-phosphorus-based linkages as taught by Kmiec II. In yet another embodiment, each RNA-type nucleotide in the mixed duplex oligonucleotide is a 2′-Substituted Nucleotide. Particularly preferred embodiments of 2′-Substituted Ribonucleotides are 2′-fluoro, 2′-methoxy, 2′-propyloxy, 2′-allyloxy, 2′-hydroxylethyloxy, 2′-methoxyethyloxy, 2′-fluoropropyloxy and 2′-trifluoropropyloxy substituted ribonucleotides. More preferred embodiments of 2′-Substituted Ribonucleotides are 2′-fluoro, 2′-methoxy, 2′-methoxyethyloxy, and 2′-allyloxy substituted nucleotides. In another embodiment the mixed duplex oligonucleotide is linked by unsubstituted phosphodiester bonds.

Although mixed duplex oligonucleotide having only a single type of 2′-substituted RNA-type nucleotide are more conveniently synthesized, the methods of the invention can be practiced with mixed duplex oligonucleotides having two or more types of RNA-type nucleotides. The function of an RNA segment may not be affected by an interruption caused by the introduction of a deoxynucleotide between two RNA-type trinucleotides, accordingly, the term RNA segment encompasses such an “interrupted RNA segment.” An uninterrupted RNA segment is termed a contiguous RNA segment. In an alternative embodiment an RNA segment can contain alternating RNase-resistant and unsubstituted 2′-OH nucleotides. The mixed duplex oligonucleotides preferably have fewer than 100 nucleotides and more preferably fewer than 85 nucleotides, but more than 50 nucleotides. The first and second strands are Watson-Crick base paired. In one embodiment the strands of the mixed duplex oligonucleotide are covalently bonded by a linker, such as a single stranded hexa, penta or tetranucleotide so that the first and second strands are segments of a single oligonucleotide chain having a single 3′ and a single 5′ end. The 3′ and 5′ ends can be protected by the addition of a “hairpin cap” whereby the 3′ and 5′ terminal nucleotides are Watson-Crick paired to adjacent nucleotides. A second hairpin cap can, additionally, be placed at the junction between the first and second strands distant from the 3′ and 5′ ends, so that the Watson-Crick pairing between the first and second strands is stabilized.

The first and second strands contain two regions that are homologous with two fragments of the target EPSPS gene, i.e., have the same sequence as the target gene. A homologous region contains the nucleotides of an RNA segment and may contain one or more DNA-type nucleotides of connecting DNA segment and may also contain DNA-type nucleotides that are not within the intervening DNA segment. The two regions of homology are separated by, and each is adjacent to, a region having a sequence that differs from the sequence of the target gene, termed a “heterologous region.” The heterologous region can contain one, two or three mismatched nucleotides. The mismatched nucleotides can be contiguous or alternatively can be separated by one or two nucleotides that are homologous with the target gene. Alternatively, the heterologous region can also contain an insertion or one, two, three or of five or fewer nucleotides. Alternatively, the sequence of the mixed duplex oligonucleotide may differ from the sequence of the target gene only by the deletion of one, two, three, or five or fewer nucleotides from the mixed duplex oligonucleotide. The length and position of the heterologous region is, in this case, deemed to be the length of the deletion, even though no nucleotides of the mixed duplex oligonucleotide are within the heterologous region. The distance between the fragments of the target gene that are complementary to the two homologous regions is identically the length of the heterologous region when a substitution or substitutions is intended. When the heterologous region contains an insertion, the homologous regions are thereby separated in the mixed duplex oligonucleotide farther than their complementary homologous fragments are in the gene, and the converse is applicable when the heterologous region encodes a deletion.

The RNA segments of the mixed duplex oligonucleotides are each a part of a homologous region, i.e., a region that is identical in sequence to a fragment of the target gene, which segments together preferably contain at least 13 RNA-type nucleotides and preferably from 16 to 25 RNA-type nucleotides or yet more preferably 18-22 RNA-type nucleotides or most preferably 20 nucleotides. In one embodiment, RNA segments of the homology regions are separated by and adjacent to, i.e., “connected by” an intervening DNA segment. In one embodiment, each nucleotide of the heterologous region is a nucleotide of the intervening DNA segment. An intervening DNA segment that contains the heterologous region of a mixed duplex oligonucleotide is termed a “mutator segment.”

The change to be introduced into the target EPSPS gene is encoded by the heterologous region. The change to be introduced into the EPSPS gene may be a change in one or more bases of the EPSPS gene sequence that changes the native amino acid in that position to the desired amino acid.

In another embodiment of the present invention, the recombinagenic oligonucleobase is a single stranded oligodeoxynucleotide mutational vector or SSOMV, which is disclosed in International Patent Application PCT/US00/23457, which is incorporated herein by reference in its entirety. The sequence of the SSOMV is based on the same principles as the mutational vectors described in U.S. Pat. Nos. 5,756,325; 5,871,984; 5,760,012; 5,888,983; 5,795,972; 5,780,296; 5,945,339; 6,004,804; and 6,010,907 and in International Publication Nos. WO 98/49350; WO 99/07865; WO 99/58723; WO 99/58702; WO 99/40789; U.S. Pat. No. 6,870,075; and US Published Patent Application 20030084473. The sequence of the SSOMV contains two regions that are homologous with the target sequence separated by a region that contains the desired genetic alteration termed the mutator region. The mutator region can have a sequence that is the same length as the sequence that separates the homologous regions in the target sequence, but having a different sequence. Such a mutator region will cause a substitution.

The nucleotides of the SSOMV are deoxyribonucleotides that are linked by unmodified phosphodiester bonds except that the 3′ terminal and/or 5′ terminal internucleotide linkage or alternatively the two 3′ terminal and/or 5′ terminal internucleotide linkages can be a phosphorothioate or phosphoamidate. As used herein an internucleotide linkage is the linkage between nucleotides of the SSOMV and does not include the linkage between the 3′ end nucleotide or 5′ end nucleotide and a blocking substituent, see supra. In a specific embodiment the length of the SSOMV is between 21 and 55 deoxynucleotides and the lengths of the homology regions are, accordingly, a total length of at least 20 deoxynucleotides and at least two homology regions should each have lengths of at least 8 deoxynucleotides.

The SSOMV can be designed to be complementary to either the coding or the non-coding strand of the target gene. When the desired mutation is a substitution of a single base, it is preferred that both the mutator nucleotides be a pyrimidine. To the extent that is consistent with achieving the desired functional result it is preferred that both the mutator nucleotide and the targeted nucleotide in the complementary strand be pyrimidines. Particularly preferred are SSOMV that encode transversion mutations, i.e., a C or T mutator nucleotide is mismatched, respectively, with a C or T nucleotide in the complementary strand.

In addition to the oligodeoxynucleotide the SSOMV can contain a 5′ blocking substituent that is attached to the 5′ terminal carbons through a linker. The chemistry of the linker is not critical other than its length, which should preferably be at least 6 atoms long and that the linker should be flexible. A variety of non-toxic substituents such as biotin, cholesterol or other steroids or a non-intercalating cationic fluorescent dye can be used. Particularly preferred as reagents to make SSOMV are the reagents sold as Cy3™ and Cy5™ by Glen Research, Sterling Va., which are blocked phosphoroamidites that upon incorporation into an oligonucleotide yield 3,3,3′,3′-tetramethyl N,N′-isopropyl substituted indomonocarbocyanine and indodicarbocyanine dyes, respectively. Cy3 is the most preferred. When the indocarbocyanine is N-oxyalkyl substituted it can be conveniently linked to the 5′ terminal of the oligodeoxynucleotide through as a phosphodiester with a 5′ terminal phosphate. The chemistry of the dye linker between the dye and the oligodeoxynucleotide is not critical and is chosen for synthetic convenience. When the commercially available Cy3 phosphoramidite is used as directed the resulting 5′ modification consists of a blocking substituent and linker together which are a N-hydroxypropyl, N′-phosphatidylpropyl 3,3,3′,3′-tetramethyl indomonocarbocyanine.

In a preferred embodiment the indocarbocyanine dye is tetra substituted at the 3 and 3′ positions of the indole rings. Without limitation as to theory these substitutions prevent the dye from being an intercalating dye. The identity of the substituents at these positions are not critical. The SSOMV can in addition have a 3′ blocking substituent. Again the chemistry of the 3′ blocking substituent is not critical.

In another preferred embodiment the recombinageneic oligonucleotide is a single-stranded oligodeoxynucleotide having a 3′ end nucleotide, a 5′ end nucleotide, having at least 25 deoxynucleotides and not more than 65 deoxynucleotides, and having a sequence comprising at least two regions each of at least 8 deoxynucleotides that are each, respectively, identical to at least two regions of the targeted chromosomal gene, which regions together are at least 24 nucleotides in length, and which regions are separated by at least one nucleotide in the sequence of the targeted chromosomal gene or in the sequence of the oligodeoxynucleotide or both such that the sequence of the oligodeoxynucleotide is not identical to the sequence of the targeted chromosomal gene. See U.S. Pat. No. 6,271,360 which is incorporated herein by reference.

Microcarriers and Microfibers

The use of metallic microcarriers (microspheres) for introducing large fragments of DNA into plant cells having cellulose cell walls by projectile penetration is well known to those skilled in the relevant art (henceforth biolistic delivery). U.S. Pat. Nos. 4,945,050; 5,100,792 and 5,204,253 describe general techniques for selecting microcarriers and devices for projecting them. U.S. Pat. Nos. 5,484,956 and 5,489,520 describe the preparation of fertile transgenic corn using microprojectile bombardment of corn callus tissue. The biolistic techniques are also used in transforming immature corn embryos.

Specific conditions for using microcarriers in the methods of the present invention are described in International Publication WO 99/07865. In an illustrative technique, ice cold microcarriers (60 mg/ml), mixed duplex oligonucleotide (60 mg/ml) 2.5 M CaCl.sub.2 and 0.1 M spermidine are added in that order; the mixture is gently agitated, e.g., by vortexing, for 10 minutes and let stand at room temperature for 10 minutes, whereupon the microcarriers are diluted in 5 volumes of ethanol, centrifuged and resuspended in 100% ethanol. Good results can be obtained with a concentration in the adhering solution of 8-10 μg/μl microcarriers, 14-17 μg/ml mixed duplex oligonucleotide, 1.1-1.4 M CaCl.sub.2 and 18-22 mM spermidine. Optimal results were observed under the conditions of 8 μg/μl microcarriers, 16.5 μg/ml mixed duplex oligonucleotide, 1.3 M CaCl.sub.2 and 21 mM spermidine.

Recombinagenic oligonucleobases can also be introduced into plant cells for the practice of the present invention using microfibers to penetrate the cell wall and cell membrane. U.S. Pat. No. 5,302,523 to Coffee et al. describes the use of 30.times.0.5 μm and 10.times.0.3 μm silicon carbide fibers to facilitate transformation of suspension maize cultures of Black Mexican Sweet. Any mechanical technique that can be used to introduce DNA for transformation of a plant cell using microfibers can be used to deliver recombinagenic oligonucleobases for use in making the present EPSPS mutants. The process disclosed by Coffee et al in U.S. Pat. No. 5,302,523 can be employed with regenerable plant cell materials to introduce the present recombinagenic oligonucleobases to effect the mutation of the EPSPS gene whereby a whole mutated plant can be recovered that exhibits the glyphosate resistant phenotype.

An illustrative technique for microfiber delivery of a recombinagenic oligonucleobase is as follows: Sterile microfibers (2 μg) are suspended in 150 μl of plant culture medium containing about 10.mu.g of a mixed duplex oligonucleotide. A suspension culture is allowed to settle and equal volumes of packed cells and the sterile fiber/nucleotide suspension are vortexed for 10 minutes and plated. Selective media are applied immediately or with a delay of up to about 120 hours as is appropriate for the particular trait.

Electroporation

In an alternative embodiment, the recombinagenic oligonucleobases can be delivered to the plant cell by electroporation of a protoplast derived from a plant part according to techniques that are well-known to one of ordinary skill in the art. See, e.g., Gallois et al., 1996, in Methods in Molecular Biology 55:89-107, Humana Press, Totowa, N.J.; Kipp et al., 1999, in Methods in Molecular Biology 133:213-221, Humana Press, Totowa, N.J.

Recombinagenic oligonucleobases can also be introduced into microspores by electroporation. Upon release of the tetrad, the microspore is uninucleate and thin-walled. It begins to enlarge and develops a germpore before the exine forms. A microspore at this stage is potentially more amenable to transformation with exogenous DNA than other plant cells. In addition, microspore development can be altered in vitro to produce either haploid embryos or embryogenic callus that can be regenerated into plants (Coumans et al., Plant Cell Rep. 7:618-621, 1989; Datta et al., Plant Sci. 67:83-88, 1990; Maheshwari et al., Am. J Bot. 69:865-879, 1982; Schaeffer, Adv. In Cell Culture 7:161-182, 1989; Swanson et al., Plant Cell Rep. 6:94-97, 1987). Thus, transformed microspores can be regenerated directly into haploid plants or dihaploid fertile plants upon chromosome doubling by standard methods. See also co-pending application U.S. Ser. No. 09/680,858 entitled Compositions and Methods for Plant Genetic Modification which is incorporated herein by reference.

Microspore electroporation can be practiced with any plant species for which microspore culture is possible, including but not limited to plants in the families Graminae, Leguminoceae, Cruciferaceae, Solanaceac, Cucurbitaceae, Rosaccae, Poaceae, Lilaceae, Rutaceae, Vitaceae, including such species as corn (Zea mays), wheat (Triticum aestivum), rice (Oryza sativa), oats, barley, canola (Brassica napus, Brassica rapa, Brassica oleracea, and Brassicajuncea), cotton (Gossypium hirsuitum L.), various legume species (e.g., soybean [Glycine max], pea [Pisum sativum], etc.), grapes [Vitis vinifera], and a host of other important crop plants. Microspore embryogenesis, both from anther and microspore culture, has been described in more than 170 species, belonging to 68 genera and 28 families of dicotyledons and monocotyledons (Raghavan, Embryogenesis in Agniosperms: A Developmental and Experimental Study, Cambridge University Press, Cambridge, England, 1986; Rhagavan, Cell Differentiation 21:213-226, 1987; Raemakers et al., Euphytica 81:93-107, 1995). For a detailed discussion of microspore isolation, culture, and regeneration of double haploid plants from microspore-derived embryos [MDE] in Brassica napus L., see Nehlin, The Use of Rapeseed (Brassica napus L.) Microspores as a Tool for Biotechnological Applications, doctoral thesis, Swedish University of Agricultural Sciences, Uppsala, Sweden, 1999; also Nehlin et al., Plant Sci. 111:219-227, 1995, and Nehlin et al., Plant Sci. 111:219-227, 1995). Chromosome doubling from microspore or anther culture is a well-established technique for production of double-haploid homozogous plant lines in several crops (Heberle-Bors et al., In vitro pollen cultures: Progress and perspectives. In: Pollen Biotechnology. Gene expression and allergen characterization, vol. 85-109, ed. Mohapatra, S. S., and Knox, R. B., Chapman and Hall, New York, 1996).

Microspore electroporation methods are described in Jardinaud et al., Plant Sci. 93:177-184, 1993, and Fennell and Hauptman, Plant Cell Reports 11:567-570, 1992. Methods for electroporation of MDON into plant protoplasts can also be adapted for use in microspore electroporation.

Whiskers and Microinjection

In yet another alternative embodiment, the recombinagenic oligonucleobase can be delivered to the plant cell by whiskers or microinjection of the plant cell. The so called whiskers technique is performed essentially as described in Frame et al., 1994, Plant J. 6:941-948. The recombinagenic oligonucleobase is added to the whiskers and used to transform the plant cells. The recombinagenic oligonucleobase may be co-incubated with plasmids comprising sequences encoding proteins capable of forming recombinase complexes in plant cells such that recombination is catalyzed between the oligonucleotide and the target sequence in the EPSPS gene.

Selection of Glyphosate Resistant Plants

Plants or plant cells can be tested for resistance or tolerance to a phosphonomethylglycine herbicide using commonly known methods in the art, e.g., by growing the plant or plant cell in the presence of a phosphonomethylglycine herbicide and measuring the rate of growth as compared to the growth rate of control plants in the absence of the herbicide. In the case of glyphosate concentrations of from about 0.01 to about 20 mM are employed in selection medium.

The following examples illustrate the practice of the present invention but should not be construed as limiting its scope.

EXAMPLE 1 P178A Mutants in Brassica napus (Canola)

The following genoplast (recombinagenic oligonucleobase) was made to make a P178A change in Brassica napus (canola) germplasm:

SEQ ID 1: VATGCAGGAACAGCCATGCGTTCACTTACGGCTGCAGTTACTH wherein V is a fluorescent dye (V=Cy3) and H is a reverse nucleotide or reverse base (H=3′DMTdCCPG). The underlined nucelobases represent the heterologous region (codon) where the mutation occurs in the canola genome, ie, A. The genoplast is made according to well known techniques and the genoplast is preferably delivered into a canola plant cell via microparticle bombardment, ie, biolistics. Canola plants regenerated that contain the P178A mutant are resistant to glyphosate when applied at commercial rates.

EXAMPLE 2 P173A Mutants in Oryza sativa (Rice)

The following genoplast (recombinagenic oligonucleobase) was made to make a P173A change in Oryza sativa (rice) germplasm:

SEQ ID 2: VGGAACGCTGGAACTGCAATGCGAGCATTGACAGCAGCCGTGACTGCH wherein V is a fluorescent dye (V=Cy3) and H is a reverse nucleotide or reverse base (H=3′DMTdCCPG). The underlined nucleobases represent the heterologous region (codon) where the mutation occurs in the rice genome, ie, A. The genoplast is made according to well known techniques and the genoplast is preferably delivered into a rice plant cell via microparticle bombardment, ie, biolistics. Rice plants regenerated that contain the P173A mutant are resistant to glyphosate when applied at commercial rates.

EXAMPLE 3 E Coli and Arabidposis Mutants

The following table lists the EPSPS mutations in E coli (Area) and Arabidopsis NM 130093 that produce a glyphosate resistant phenotype. The specific codon change is indicated in the right column.

ARABIDOPSIS E. COLI NM 130093 MUTATION 1. T₉₇ → A₉₇ T178A ACA → GCA 2. L₈₂ →S₈₂ F159S TTC → TCC 3. P₁₀₁ → C₁₀₁ P182C CCA → TGC 4. T₉₇; P₁₀₁ → I₉₇; A₁₀₁ T178I; P182A (T -> I) ACA → ATA; (P -> A) CCA -> GCA 5. *N₁₉₄ → A₁₉₄ N193A AAC → GCC 6. T₉₇; P₁₀₁ → A₉₇; A₁₀₁ T178A; P182A (T -> A) ACA → GCA; (P -> A) CCA -> GCA 7. T₉₇; P₁₀₁ → A₉₇; T₁₀₁ T178A; P182T (T -> A) ACA → GCA; (P -> T) CCA → ACA 8. L₈₂; P₁₀₁ → S₈₂; A₁₀₁ F159S; P182A (F -> S) TTC → TCC; (P -> A) CCA -> GCA 9. L₈₂; P₁₀₁ → S₈₂; T₁₀₁ F159S; P182T (F -> S) TTC → TCC; (P -> T) CCA -> ACA *No true homologous amino acid in E. coli. The closest homologous amino acid in E. coli is N111. Also note that the native E coli has an L in the 82 position and the analogous amino acid in Arabodposis at position 159 is F

The following listing (a-g) shows in more detail the present mutations. All references to “Arabidopsis” are to the Arabidopsis gene NM 130093. The sequences are the gene sequences of the native EPSPS gene (top) and the mutated EPSPS gene (bottom). The mutated codon is bolded and underlined where the changed nucleotide is represented by a lower case letter. Sections a-g disclose SEQ ID NOS: 3-16, respectively, in order of appearance.

a. T178A E. COLI ARABIDOPSIS MUTATION 1. T₉₇ → A₉₇ T178A ACA → GCA CTTTACCTCGGTAATGCAGGA ACA GCAATGCGTCCACTTACC CTTTACCTCGGTAATGCAGGA gCA GCAATGCGTCCACTTACC b. F159S E. COLI ARABIDOPSIS MUTATION 2. L₈₂ → S₈₂ F1598 TTC → TCC GGATGTGGCGGGATA TTC CCAGCTTCCATAGATTC GGATGTGGCGGGATA TcC CCAGCTTCCATAGATTC c. P101C E. COLI ARABIDOPSIS MUTATION 3. P₁₀₁ → C₁₀₁  P182C CCA → TGC GCAGGAACAGCAATGCGT CCA CTTACCGCTGCGGTC GCAGGAACAGCAATGCGT tgc CTTACCGCTGCGGTC d. T178I; P182A E. COLI ARABIDOPSIS MUTATION 4. T₉₇; P₁₀₁ → I₉₇; A₁₀₁ T178I; P182A (T -> I) ACA → ATA; (P -> A) CCA → GCA CCTCGGTAATGCAGGA ACA GCAATGCGT CCA CTTAC CCTCGGTAATGCAGGA AtA GCAATGCGT gCA CTTAC e. N193A E. COLI ARABIDOPSIS MUTATION 5.  *N₁₉₃ → A₁₉₃ N193A AAC → GCC GGTCACTGCTGCAGGTGGA AAC GCAAGTTATGTGCTTG GGTCACTGCTGCAGGTGGA gcC GCAAGTTATGTGCTTG f. T178A; P182A E. COLI ARABIDOPSIS MUTATION 6. T₉₇; P₁₀₁ → A₉₇; A₁₀₁ T178A; P182A (T → A) ACA → GCA; (P → A) CCA → GCA CCTCGGTAATGCAGGA ACA GCAATGCGT CCA CTTAC CCTCGGTAATGCAGGA gCA GCAATGCGT gCA CTTAC g. T178A; P182T E. COLI ARABIDOPSIS MUTATION 7.  T₉₇; P₁₀₁ → A₉₇; T₁₀₁ T178A; P182T (T → A) ACA → GCA; (P → T) CCA → ACA CCTCGGTAATGCAGGA ACA GCAATGCGT CCA CTTAC CCTCGGTAATGCAGGA gCA GCAATGCGT aCA CTTAC 

We claim:
 1. An herbicide resistant plant that comprises a genomic EPSPS gene that expresses a EPSPS protein that is mutated at amino acid positions Thr₁₇₉ and Pro₁₈₃ in an Arabidopsis EPSPS protein (SEQ ID NO: 19) or at an analogous amino acid residue in an EPSPS homolog, wherein Thr₁₇₉ is changed to Ile and Pro₁₈₃ is changed to Leu or Cys.
 2. A method for producing a non-transgenic, herbicide resistant or tolerant plant comprising: introducing into plant cells a recombinagenic oligonucleobase with a targeted mutation in the EPSPS gene to produce plant cells with a mutant genomic EPSPS gene that expresses a EPSPS protein that is mutated at amino acid positions Thr₁₇₉ and Pro₁₈₃ in an Arabidopsis EPSPS protein (SEQ ID NO: 19) or at an analogous amino acid residue in an EPSPS homolog, wherein Thr₁₇₉ is changed to Ile and Pro₁₈₃ is changed to Leu or Cys; selecting a plant cell exhibiting improved tolerance to glyphosate as compared to a corresponding wild-type plant cell; and regenerating a non-transgenic herbicide resistant or tolerant plant having a mutated EPSPS gene from said selected plant cell. 